A single nucleotide polymorphism in SPATA17 may be a genetic risk factor for Japanese patients with meiotic arrest

Genetic mechanisms have been implicated as a cause of some cases of male infertility. Recently, 10 novel genes involved in human spermatogenesis were identified by microarray analysis of human testicular tissue. One of these is spermatogenesis-associated 17 (SPATA17). To investigate whether defects...

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Detalhes bibliográficos
Main Authors: Miyamoto, Toshinobu, Tsujimura, Akira, Miyagawa, Yasushi, Koh, Eitetsu, Sakugawa, Naoko, Miyakawa, Hiroe, Sato, Hisashi, Namiki, Mikio, Okuyama, Akihiko, Sengoku, Kazuo
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2009
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3735008/
https://ncbi.nlm.nih.gov/pubmed/19483714
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/aja.2009.30
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